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血清氯水平与肺动脉高压患者的生存情况相关。

Serum Chloride Levels Track With Survival in Patients With Pulmonary Arterial Hypertension.

机构信息

Pathobiology Department, Cleveland Clinic, Cleveland, OH.

Internal Medicine Residency Program, Medicine Institute, Cleveland Clinic, Cleveland, OH.

出版信息

Chest. 2018 Sep;154(3):541-549. doi: 10.1016/j.chest.2018.04.022. Epub 2018 Apr 24.

Abstract

BACKGROUND

Serum chloride is an important homeostatic biomarker in left heart failure, with significant prognostic implications. The impact of serum chloride in the long-term survival of patients with pulmonary arterial hypertension (PAH) is unknown. We tested whether serum chloride levels are associated with long-term survival in patients with PAH.

METHODS

We included patients with idiopathic or heritable PAH who had a basic metabolic panel performed at the time of their diagnostic right heart catheterization. Laboratory results were recorded both at diagnosis and 6-month follow-up.

RESULTS

We included 277 patients, mean age 51 ± 18 years and 73% women, of whom 254 had a follow-up electrolyte determination at 6 months. Serum chloride was 102.9 ± 3.9 mM/L at diagnosis. A serum chloride ≤ 100 mM/L was noted in 65 (24%) and 53 (21%) patients at diagnosis and 6 months, respectively. Patients with serum chloride ≤ 100 mM/L at 6 months tracked with increase mortality when adjusted by age, sex, pulmonary vascular resistance, diuretics or prostacyclin analogs usage, and serum creatinine and sodium at 6 months (hazard ratio, 1.83; 95% CI, 1.11-3.00). This group of patients was older, with decreased functional capacity, had worse renal function, took more diuretics, had higher pulmonary artery wedge pressure but lower mean pulmonary artery pressure, transpulmonary gradient, and pulmonary vascular resistance.

CONCLUSIONS

Serum chloride at 6 months from the PAH diagnosis is a strong and independent predictor of mortality in patients with idiopathic or heritable PAH, even after adjusting serum sodium, renal function, diuretic, and prostacyclin analog usage.

摘要

背景

血清氯是左心衰竭的一种重要的体内平衡生物标志物,具有重要的预后意义。血清氯在肺动脉高压(PAH)患者的长期生存中的影响尚不清楚。我们检测了血清氯水平与 PAH 患者长期生存的关系。

方法

我们纳入了诊断为特发性或遗传性 PAH 的患者,他们在诊断性右心导管检查时进行了基本代谢小组检查。记录了实验室结果,包括在诊断时和 6 个月随访时的结果。

结果

我们纳入了 277 名患者,平均年龄 51 ± 18 岁,73%为女性,其中 254 名患者在 6 个月时进行了电解质随访。诊断时血清氯为 102.9 ± 3.9 mM/L。诊断时和 6 个月时分别有 65(24%)和 53(21%)名患者的血清氯≤100 mM/L。在调整年龄、性别、肺血管阻力、利尿剂或前列环素类似物的使用以及 6 个月时的血清肌酐和钠后,6 个月时血清氯≤100 mM/L 的患者死亡率升高(危险比,1.83;95%置信区间,1.11-3.00)。这组患者年龄较大,运动能力下降,肾功能更差,使用了更多的利尿剂,肺动脉楔压更高,但平均肺动脉压、跨肺梯度和肺血管阻力更低。

结论

PAH 诊断后 6 个月的血清氯是特发性或遗传性 PAH 患者死亡率的一个强有力的独立预测因素,甚至在调整血清钠、肾功能、利尿剂和前列环素类似物的使用后也是如此。

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